Catalog Number

8836.017

Brand Name

NA

Version/Model Number

8836017

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 26, 2016

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

GCM

Product Code Name

ENDOSCOPE, RIGID

Public Device Record Key

f07921c6-2bb3-4419-9371-27c6c29f683e

Public Version Date

June 16, 2022

Public Version Number

3

DI Record Publish Date

September 26, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-